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Yohimbe bark. Group: Biochemicals. Alternative Names: Yohimbine. Grades: Highly Purified. CAS No. 146-48-5. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences.
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Yohimbe Extract
Yohimbe Extract. Applications: Used for men health care products, dietary supplements, treat sexual impotence and sexual dysfunction. Group: Others. Synonyms: Yohimbe Extract; 65-19-0; Corynante Yohimbe. CAS No. 65-19-0. Purity: 8% Yohimbine by HPLC. Appearance: Red brown fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Bark. Species: Corynante Yohimbe. Yohimbe Extract; 65-19-0; Corynante Yohimbe; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-077.
10,11-Dimethoxy-17-epi-alpha-yohimbine
10,11-Dimethoxy-17-epi-alpha-yohimbine is a natural compound aiding in studying ailments such as erectile dysfunction, anxiety and depression. It serves as a discriminating alpha-2-adrenergic antagonist. Grades: > 95%. CAS No. 84667-06-1. Molecular formula: C23H30N2O5. Mole weight: 414.49.
2,3-Dihydro-1,4-benzodioxin-2-carboximidic Acid Ethyl Ester Hydrochloride is an intermediate in the synthesis of Idazoxan Hydrochloride (I506800), which is an α-adrenoceptor antagonist; in rat brain Idazoxan is a pure antagonist and it has a selectivity for α2- over α1-receptors markedly superior to Piperoxane, Yohimbine, or Rauwolscine. Antiparkinsonian. Group: Biochemicals. Grades: Highly Purified. CAS No. 79944-55-1. Pack Sizes: 100mg, 250mg. Molecular Formula: C11H13NO3; HCl, Molecular Weight: 207.233645999999. US Biological Life Sciences.
Worldwide
2-Propen-1,1,2,3,3-d5-1-ol
2-Propen-1,1,2,3,3-d5-1-ol is isotopically labelled form of Allyl Alcohol, which is used in the synthesis of yohimbinoid alkaloids venenatine and alstovenine. Also used in the synthesis of polycyclic alkaloid (-)-nakadomarin A. Group: Biochemicals. Grades: Highly Purified. CAS No. 102910-30-5. Pack Sizes: 5mg, 10mg. Molecular Formula: C3HD5O. US Biological Life Sciences.
Allyl Alcohol is used in the synthesis of yohimbinoid alkaloids venenatine and alstovenine. Also used in the synthesis of (-)-nakadomarin A, a polycyclic alkaloid. Group: Biochemicals. Alternative Names: 2-Propen-1-ol;1-Hydroxy-2-propene; 1-Propen-3-ol; 2-Propenol; 2-Propenyl Alcohol; 3-Hydroxy-1-propene; 3-Hydroxypropene; Allylic Alcohol; NSC 6526; Shell Unkrauttod A; Vinylcarbinol. Grades: Highly Purified. CAS No. 107-18-6. Pack Sizes: 10g. US Biological Life Sciences.
Deserpidine is an antihypertensive drug related to Reserpine. It is naturally found in Rauvolfia spp. Deserpidine is a competitive ACE (angiotensin converting enzyme) inhibitor. Deserpidine can block the conversion of angiotensin I to angiotensin II as a potent vasoconstrictor through competing with angiotensin I for ACE. Reduced level of serum angiotensin II leads to a decrease in blood pressure. Deserpidine can also decrease angiotensin II-induced aldosterone secretion by the adrenal cortex. Uses: Antihypertensive drug. Synonyms: (3β, 16β, 17α, 18β, 20α)-17-methoxy-18-[(3, 4, 5-trimethoxybenzoyl)oxy]yohimban-16-carboxylic Acid Methyl Ester; Deserpidic Acid Methyl Ester 3,4,5-Trimethoxybenzoate; Deserpidin; 1-Demethoxyreserpine; 11-Desmethoxyreserpine; Canescin; Canescine; Canescine (Rauwolfia); Harmonyl; NSC 72138; Raunormin; Raunormine; Recanescin; Recanescine; Reserpidine. Grades: 95%. CAS No. 131-01-1. Molecular formula: C32H38N2O8. Mole weight: 578.66.
A cell-permeable quinolinimine compound that acts as a selective, potent blocker of G-protein coupled receptors (GPCR) that contain a constrained eighth helix (H8). The inhibition is selective and blocks G-protein signaling mediated via Gaq, but not Ga12. A non-orthosteric antagonist of PAR1 (IC50=4uM) that is shown to inhibit PAR1 and CCR-4 induced platelet aggregation without affecting PAR4 mediated aggregation. Shown to inhibit thrombus formation following vascular injury (IC50 ~1mg/kg). Also acts as a potent, non-competitive blocker of a2A-adrenergic receptors (IC50=2.5uM as shown by a decrease in 3H-yohimbine binding). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Reserpine derivative, an alkaloid found in Rauwolfia. Group: Biochemicals. Alternative Names: 18 β-Hydroxy-11,17α-dimethoxy-3 β,20α-yohimban-16 β-carboxylic Acid Methyl, p-Bromobenzenesulfonate Ester. Grades: Highly Purified. CAS No. 1262-67-5. Pack Sizes: 2.5mg. US Biological Life Sciences.
Rauwolscine is a selective α2-adrenoceptor antagonist that inhibits tumor growth and induces apoptosis [1]. Uses: Scientific research. Group: Natural products. Alternative Names: α-Yohimbine; Corynanthidine; Isoyohimbine. CAS No. 131-03-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-12710.
Rauwolscine hydrochloride
Rauwolscine hydrochloride is a potent and specific α2 adrenergic receptor antagonist with a K i of 12 nM. Uses: Scientific research. Group: Natural products. Alternative Names: α-Yohimbine hydrochloride; Corynanthidine hydrochloride; Isoyohimbine hydrochloride. CAS No. 6211-32-1. Pack Sizes: 1 mg. Product ID: HY-12710A.
Rauwolscine hydrochloride
Rauwolscine hydrochloride is the hydrochloride salt of Rauwolscine which is a potent, reversible and specific α2 adrenergic receptor antagonist with a Ki values are 3.5, 4.6, and 0.6 nM at cloned human α2A-AR, α2B-AR, and α2C-AR adrenoceptors, respectively. It also acts as a 5-HT2B receptor antagonist and has the function to modulate mood. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: methyl (1S,15S,18S,19S,20S)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate;hydrochloride; alpha-Yohimbine hydrochloride; Fauwolscine, hydrochloride; alpha-Yohimbin hydrochloride; NSC 407307; Rauwolscine (hydrochloride); Methyl (16beta,17alpha,20alpha)-17-hydroxyyohimban-16-carboxylate hydrochloride. CAS No. 6211-32-1. Molecular formula: C21H27ClN2O3. Mole weight: 390.9.
Reserpic Acid Methyl Ester
Reserpine derivative, an alkaloid found in Rauwolfia. Group: Biochemicals. Alternative Names: Methyl reserpate; Methyl reserpinolate; NSC 81464; (3 β,16 β,17α,18 β,20α)-18-Hydroxy-11,17-dimethoxy-yohimban-16-carboxylic Acid Methyl Ester. Grades: Highly Purified. CAS No. 2901-66-8. Pack Sizes: 5mg. US Biological Life Sciences.
Strengthening muscular tension, increasing energy metabolism of human body. Group: Material of medical care. Alternative Names: yohimbine extractive. CAS No. 65-19-0. Molecular formula: C21H26N2O3·HCL. Mole weight: 390.91. Appearance: low purity: brownish red powder; white to off-white fine powde. Catalog: ACM65190.
Yohimbine HCl
Yohimbine HCl. Group: Biochemicals. Grades: Highly Purified. CAS No. 65-19-0. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: C21H26N2O3·HCl. US Biological Life Sciences.
Worldwide
Yohimbine HCL 8% & 98% HPLC
Yohimbine HCL 8% & 98% HPLC.
CA, FL & NJ
Yohimbine Hydrochloride
Indole alkaloid with α2-adrenergic blocking activity. Mydriatic. Used in the treatment of neurological disorders. Group: Biochemicals. Grades: Highly Purified. CAS No. 65-19-0. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Yohimbine Hydrochloride
Yohimbine hydrochloride is an alpha-2 renal adenomatase receptor inhibitor, blocking pre- and post-contact alpha-2 renal adenomatase receptors, causing the release of renal adenoma and multiple sclerosis. Uses: Scientific research. Group: Natural products. CAS No. 65-19-0. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-N0127.
A potent antagonist for alpha-2-adrenoceptors (pKi values are 8.52, 8.00 and 9.17 for human alpha-2a, alpha-2B and alpha-2C receptors respectively). Often used as pharmacological stressor in animal studies. Group: Biochemicals. Grades: Highly Purified. CAS No. 65-19-0. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Yohimbine (Methyl-13C; Methyl-D3 ester)
Isotope-labeled Metabolites2H 13C Labeled Compounds. Alternative Names: Yohimbine-[13C,D3]. CAS No. 1261254-59-4. Molecular formula: C2013CH23D3N2O3. Mole weight: 358.45. Catalog: ACM1261254594.
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